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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis, bilateral

acid maltase deficiency

acid maltase deficiency, adult

acute ataxia of childhood

acute cerebellar ataxia

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

adolescent medicine

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Alexanders disease

Alexanders disease, adult onset

alkalosis, respiratory

alpha-synuclein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement, impaired

Alzheimer's disease

amblyopia, toxic

AMPA receptor antibodies

amphiphysin antibodies

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

angiography, cerebral

angiography, posterior fossa

anterior cerebral artery

anterior cerebral artery territory infarction

anterior horn cell disease

anti GQ1b IgG antibody

antibodies to measles

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, untoward effects of

antiphospholipid antibody syndrome

antistreptolysin titer

arterial dissection

arterial dissection, carotid

arterial dissection, multiple

arterial dissection, vertebral

ataxia, acute onset

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

autoimmune basal ganglia encephalitis

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

axonal spheroid

B 12 deficiency

bacterial infection

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bent spine syndrome

bone marrow biopsy

botulinum toxin

brachial neuritis

brachial neuritis, acute

brachial plexus neuropathy

brainstem, lesion of

bulbar palsy, acute

burning paresthesia

calf hypertrophy

campylobacter infection

carbon monoxide poisoning

carcinoma of lung

cardiac arrest and resuscitation

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar lesion

cerebellar peduncle

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular disease

cerebrovascular disease, risk factors in

cervical spine injury

cervical spine manipulation

cherry red spot

cherry red spot-myoclonus syndrome

chewing, impaired

chiropractic manipulation

chorea, causes of

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

conduction block

congenital heart disease

conjunctival injection

controversies in neurology

conversion reaction

corneal reflex, abnormal

corpus callosum, lesion of

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cyclic vomiting

cystoisospora belli

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

denervation of muscle

denervation potentials

dermatomyositis

descending paralysis

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

disease modifying agents

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine depleting agents

DPPX, antibodies

DPPX, antibodies, encephalitis

dropped head syndrome

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

emergencies, neurologic

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy, post anoxic

enterovirus infection of CNS

epidemiology of neurology

Epstein-Barr virus

ethics in neurology

exercise intolerance

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

fatigable chewing

flaccid paralysis

forceps delivery

frontal lobe, atrophy

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

genu of corpus callosum

gests antagoniste

Gilles de la Tourette syndrome

glaucoma, acute

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

head injury, delayed deterioration following

headache, severe

headache, sudden onset of

hemianopia, homonymous

hemimyoclonic jerks

hemisensory loss

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

Hodgkin's disease

H-reflex testing

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydroxychloroquine

hyperosmolality

hyperventilation

hypocalcemia, causes of

hypoglycorrhachia

hypokalemic paralysis

hypoparathyroidism

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

immunologic disease

immunomodulation

inclusion bodies

inclusion bodies, intranuclear

infantile hemiplegia

infectious mononucleosis

infectious mononucleosis, neurologic findings with

injection neuropathy

intellectual deficit

intellectual deterioration

internal cerebral vein

intestinal pseudoobstruction

intracranial pressure, increased

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

jaw jerk, abnormal

Kluver-Bucy syndrome

lacunar infarction

laryngismus stridulus

laughing, pathologic

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

level of consciousness, decreased

Lewy body disease, diffuse

lid closure, weakness of

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

lumbar puncture

lupus anticoagulant

lymphoma involving CNS

lysosomal storage disease

manganese intoxication

masseter muscle wasting

McLeod syndrome

Melkersson's syndrome

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, recurrent

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

middle cerebellar peduncle, lesion

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, paramagnetic effect

MRI, spinal cord

multiple sclerosis

multiple sleep latency test

muscle atrophy, progressive

muscle hypertrophy

muscle stiffness

muscle strength, testing

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenic syndrome

myelinolysis, extrapontine

myelitis, transverse

myelopathy, chronic progressive

myeloradiculopathy

myoclonic jerks

myopathy, genetic

myopathy, metabolic

myopathy, toxic

myopathy, vacuolar

myopia, sudden onset of

myositis, ocular

nausea and vomiting

near reflex, spasm of

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

nerve conduction studies, motor

nerve root biopsy

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurofibrillary degeneration

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology, brain

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, toxic

neuropsychiatry

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitroproprionic acid

NMDA antagonists

numbness, generalized

nutritional deficiency

nystagmus, monocular

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

oculopharyngeal muscular dystrophy

old age, neurology of

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, total

oral contraceptives

oral contraceptives, cerbrovascular disease and

osmotic demyelination syndrome

otitis, neurologic complications with

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, hands

Parkinson disease

Parkinson disease, dementia with

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, hemiparesis in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, presymptomatic detection

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peptides, brain

perioral numbness

peripheral blood smear

personality change

phenothiazine, dyskinesia associated with

pigmentary retinopathy

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

positive sharp waves

post infectious cerebellar ataxia

posterior choroidal artery

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

progressive spinal muscular atrophy

protein 14-3-3, cerebrospinal fluid

protozoan infection

proximal muscle atrophy

pseudoabducens palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadrantanopsia, homonymous

quadriparesis, acute

quadriparesis, progressive

quality of life

rabies, nervous system involvement with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recombinant DNA

regional enteritis

REM sleep behavior disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

reserpine treatment in movement disorder

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

salivation, excessive

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, adult onset

seizure, children

seizure, neonatal

seizure, unknown origin

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

shell fish poisoning

single photon emission computed tomography

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

speech disorder

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, classification

standing difficulty

startle myoclonus

status epilepticus

status tetanicus

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

sugarcane, mildewed

swallow evaluation

symmetric brain lesions

synucleinopathy

systemic illness

tandem gait, ataxic

tardive akathisia

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

temporal lobe, atrophy

temporal lobe, lesion

temporalis muscle wasting

tetany, normocalcemic

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic foot response

toxic encephalopathy

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, resting

tremor, thalamic

tricyclic antidepressant

trinucleotide repeats

Trousseau's sign

ulcerative colitis

unconsciousness

upgaze, paralysis of

ventricular enlargement

vestibular migraine

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss, sudden

visuospatial disturbance

vitamin deficiency

von Bonsdorff's sign

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease

wide based gait

winging of scapula

Showing articles 1400 to 1450 of 17977 << Previous Next >>

Ocular Myasthenia:A Protean Disorder
Survey of Ophthalmology 39:169-210, Weinberg,D.A.,et al, 1994

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Movement Disorders Following Lesions of the Thalamus or Subthalamic Region
Mov Disord 9:493-507, Lee,M.S. &Marsden, C.D., 1994

Isolated Sphenoid Sinusitis: The Tornoto Hospital for Sick Children Experience and Review of the Literature
J Otolaryngol 23:36-41, Hnatuk,L.A.P.,et al, 1994

Acquired Cerebral Achromatopsia
Neuro Ophthalmol 14:31-36, Setala, K. & Vesti, E., 1994

Definitions and Classification of Tic Disorders
Arch Neurol 50:1013-1016, Fahn,S.,et al, 1993

Time of Hospital Presentation in Patients with Acute Stroke
Arch Int Med 153:2558-2560, Barsan,W.G.,et al, 1993

End-State Alzheimer's Disease:Glasgow Coma Scale and the Neurologic Examination
Arch Neurol 50:1309-1315, Benesch,C.G.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
JAMA 270:2321-2325, Babul,R.,et al, 1993

A 10-Year Experience with Postpump Chorea
Ann Neurol 34:820-826, Medlock,M.D.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Hemibody Tremor Related to Stroke
Stroke 24:2094-2096, Dethy,S.,et al, 1993

Outcome of Childhood Status Epilepticus and Lengthy Febrile Convulsions:Findings of National Cohort Study
BMJ 307:225-228, Verity,C.M.,et al, 1993

Serum Cortisol and Cerebrospinal Fluid B-Endorphins in Status Epilepticus:Their Possible Relation to Prognosis
Arch Neurol 50:689-693, Calabrese,V.P.,et al, 1993

Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993

A Controlled Trial of Diazepam Administered During Febrile Illnesses to Prevent Recurrence of Febrile Seizures
NEJM 329:79-84, Rosman,N.P.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Remission of Seizures in Untreated Epilepsy
BMJ 307:483, Keranen,T.&Riekkinen,P.J., 1993

Sleep State and the Risk of Seizure Recurrence Following a First Unprovoked Seizure in Childhood
Neurol 43:701-706, Shinnar,S.,et al, 1993

Treatment of Convulsive Status Epilepticus
Recommendations of the Epilepsy Foundation of America's Working Group on Status Epilepticus, JAMA 27, :54-859,1993., 1993

Biologic Factors as Predictors of Social Outcome of epilepsy in Intellectually Normal Children:A Population-Based Study
J Pediatr 122:869-873, Camfield,C.,et al, 1993

New-Onset Seizures in Critically Ill Patients
Neurol 43:1042-1044, Wijdicks,E.F.M.&Sharbrough,F.W., 1993

Sydenham's Chorea:Physical and Psychological Symptoms of St. Vitus Dance
Pediatrics 91:706-713, Swedo,S.E.,et al, 1993

Alternating Hemiplegia of Childhood
J Pediatr 122:673-679, Bourgeois,M.,et al, 1993

Long-Term Complications of Diabetes Mellitus
NEJM 328:1676-1685, Nathan,D.M., 1993

Contrast Agent Overdose Causing Brain Retention of Contrast, Seizures, and Parkinsonism
Neurol 43:836-838, May,E.F.,et al, 1993

Hemiplegic Migraine and Moyamoya Disease
Am J Dis Child 147:718-719, Bernstein,A.L., 1993

Longitudinal Exper with Botulinum Toxin Injections for Treat of Blepharospasm & Cervical Dystonia
Neurol 43:834-836, Jankovic,J.&Schwartz,K.S., 1993

Cortical Vascular Abnor in Synd of Celiac Disease, Epilepsy, Bilateral Occipital Calc, & Folate Deficiency
Ann Neurol 34:399-403, Bye,A.M.E.,et al, 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Isolated or Predominant Ocular Motor Nerve Palsy as a Manifestation of Brain Stem Stroke
Stroke 24:581-586, Kim,J.S.,et al, 1993

Short-Cycle Periodic Alternating (Ping-Pong) Gaze
Neurol 43:1067-1070, Ishikawa,H.,et al, 1993

Risk Factors for Parkinson's Disease
Neurol 43:1693-1697, 16411993., Hubble,J.P.,et al, 1993

Prognostic Significance of the Onset Mode in Parkinsonism
Neurol 43:829-830, Rajput,A.H.,et al, 1993

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

Progression After Chronic Manganese Exposure
Neurol 43:1479-1483, Huang,C.C.,et al, 1993

Therapy for Human Immunodeficiency Virus Infection
NEJM 328:1686-1695, Hirsch,M.S.&D'Aquila,R., 1993

The Prevalence of Metoclopramide-Induced Tardive Dyskinesia and Acute Extrapyramidal Movement Disorders
Arch Int Med 153:1469-1475, Ganzini,L.,et al, 1993

Unilateral Amnesic Stroke:Six New Cases and a Review of the Literature
Stroke 24:1033-1042, Ott,B.R.&Saver,J.L., 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Epilepsy as a Risk Factor for Submersion Injury in Children
Pediatrics 91:612-616, Biekema,D.S.,et al, 1993

Random Trial AEDs in Reducing Risk of Relapse After First Unprovoked Tonic-Clonic Seizure
First Seizure Trial Gr, Neurol 43:478-4831993., , 1993

New-Onset Seizures in an Elderly Hospitalized Population
Neurol 43:489-492, Ettinger,A.B.&Shinnar,S., 1993

Efficacy of Felbamate in Childhood Epileptic Encephalopathy (Lennox-Gestaut Syndrome)
Felbamate Study Group in Lennox-Gestaut Synd, NEJM 328:29-331993., , 1993

X-Linked Adrenoleukodystrophy:Adult Cerebral Variant
Neurol 43:1518-1522, Farrell,D.F.,et al, 1993

Showing articles 1400 to 1450 of 17977 << Previous Next >>